Journal article

Analysis of the N-terminal region of human MLKL, as well as two distinct MLKL isoforms, reveals new insights into necroptotic cell death

KH Arnež, M Kindlova, NJ Bokil, JM Murphy, MJ Sweet, G Gunčar

Bioscience Reports | Published : 2016

Abstract

The pseudokinase mixed lineage kinase domain-like (MLKL) is an essential effector of necroptotic cell death. Two distinct human MLKL isoforms have previously been reported, but their capacities to trigger cell death have not been compared directly. Herein, we examine these two MLKL isoforms, and further probe the features of the human MLKL N-terminal domain that are required for cell death. Expression in HEK293T cells of the N-terminal 201 amino acids (aa) of human MLKL is sufficient to cause cell death, whereas expression of the first 154 aa is not. Given that aa 1125 are able to initiate necroptosis, our findings indicate that the helix that follows this region restrains necroptotic activi..

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University of Melbourne Researchers

Grants

Awarded by National Health and Medical Research Council


Funding Acknowledgements

This work was supported by the Slovenian Research Agency and the Slovene Human Resources, Development and Scholarship Fund (to K. H. Arnez); the Group of Eight European Fellowship [grant number 2013002751 (to M. Kindlova)]; the National Health and Medical Research Council of Australia [grant number APP1003470 (to M. J. Sweet)]; and the National Health and Medical Research Council of Australia (Project 1057905 and IRIISS 9000220) and the Victorian Operational Infrastructure Support (to J. M. Murphy).